-
Congenital ichthyosiform erythroderma, also
known as
nonbullous congenital ichthyosiform erythroderma,: 484 is a rare type of the
ichthyosis family of...
- may be
required as well.
Ichthyosis Congenital ichthyosiform erythroderma Bullous congenital ichthyosiform erythroderma Larrègue M,
Ottavy N, Bressieux...
- STS
Harlequin ichthyosis 242500
Autosomal recessive ABCA12
Congenital ichthyosiform erythoderma 242100
Autosomal recessive TGMI1, NIPAL4, ALOX12B, ALOXE3...
-
Nonbullous ichthyosiform erythroderma also
known as
bullous epidermis ichthyosis (BEI),
epidermolytic hyperkeratosis (EHK),
bullous congenital ichthyosiform erythroderma...
- An
adverse drug
reaction (ADR) is a harmful,
unintended result caused by
taking medication.: 1.1
Adverse Drug
Reaction (ADR) ADRs may
occur following...
-
Congenital hemidysplasia with
ichthyosiform erythroderma and limb
defects (also
known as "CHILD syndrome") is a
genetic disorder with
onset at
birth seen...
-
which are the most
common morphology of
cutaneous sarcoidosis.: 708
Ichthyosiform sarcoidosis is a
cutaneous condition resembling ichthyosis vulgaris...
- Keratitis–ichthyosis–deafness
syndrome (KID syndrome), also
known as
ichthyosiform erythroderma,
corneal involvement, and deafness,
presents at birth/infancy...
-
acronym CHIME is
based on its main symptoms: colobomas,
heart defects,
ichthyosiform dermatosis,
intellectual disability, and
either ear
defects or epilepsy...
- Less
severe mutations result in a
collodion membrane and
congenital ichthyosiform erythroderma-like presentation. ABCA12 is an ATP-binding c****ette transporter...
